Varian Universal Interstitial Cylinder Set GM11013300

GUDID 00816389027862

Contains: GM11013310-00816389027879, GM11013320-00816389027886, GM11013330-00816389027893, GM11013340-00816389027909

VARIAN MEDICAL SYSTEMS, INC.

Vaginal brachytherapy system applicator, remote-afterloading Vaginal brachytherapy system applicator, remote-afterloading Vaginal brachytherapy system applicator, remote-afterloading Vaginal brachytherapy system applicator, remote-afterloading Vaginal brachytherapy system applicator, remote-afterloading Vaginal brachytherapy system applicator, remote-afterloading Vaginal brachytherapy system applicator, remote-afterloading Vaginal brachytherapy system applicator, remote-afterloading Vaginal brachytherapy system applicator, remote-afterloading Vaginal brachytherapy system applicator, remote-afterloading Vaginal brachytherapy system applicator, remote-afterloading Vaginal brachytherapy system applicator, remote-afterloading Vaginal brachytherapy system applicator, remote-afterloading Vaginal brachytherapy system applicator, remote-afterloading Vaginal brachytherapy system applicator, remote-afterloading
Primary Device ID00816389027862
NIH Device Record Keya51de09b-c60c-4266-aafb-b85da43ac99d
Commercial Distribution StatusIn Commercial Distribution
Brand NameVarian Universal Interstitial Cylinder Set
Version Model NumberGM11013300
Catalog NumberGM11013300
Company DUNS009120817
Company NameVARIAN MEDICAL SYSTEMS, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Conditional
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100816389027862 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

JAQSystem, applicator, radionuclide, remote-controlled

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00816389027862]

Dry Heat Sterilization


[00816389027862]

Dry Heat Sterilization


[00816389027862]

Dry Heat Sterilization


[00816389027862]

Dry Heat Sterilization


[00816389027862]

Dry Heat Sterilization


[00816389027862]

Dry Heat Sterilization


[00816389027862]

Dry Heat Sterilization


[00816389027862]

Dry Heat Sterilization


[00816389027862]

Dry Heat Sterilization


[00816389027862]

Dry Heat Sterilization


[00816389027862]

Dry Heat Sterilization


[00816389027862]

Dry Heat Sterilization


[00816389027862]

Dry Heat Sterilization


[00816389027862]

Dry Heat Sterilization


[00816389027862]

Dry Heat Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-03-03
Device Publish Date2021-02-23

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